Healthcare Software Development

HIPAA compliance is architected into every healthcare engagement from day one — it's not a checklist we run at the end. We implement AES-256 encryption at rest, TLS 1.2+ encryption in transit, role-based access controls with least-privilege principles, comprehensive audit logging for all PHI access, and BAA-ready infrastructure. Our teams conduct security reviews before every production deployment, including penetration testing and vulnerability scanning. We've built HIPAA-compliant systems for Abbott, clinical research platforms, patient engagement tools, and telehealth infrastructure.

Yes. We build custom integrations with Epic, Cerner (now Oracle Health), Allscripts, and other major EHR platforms using HL7 FHIR R4, C-CDA document exchange, REST APIs, and vendor-specific interfaces. Our teams handle the complexity of healthcare interoperability standards — resource mapping, data transformation, validation rules, and the 21st Century Cures Act requirements for patient data access. We also integrate with lab information systems, pharmacy platforms, and claims processing systems.

We build clinical workflow platforms, EHR integrations, patient engagement portals, telehealth and remote monitoring systems, health data analytics dashboards, revenue cycle management tools, clinical decision support systems, and medical device companion apps. We serve providers (hospitals, health systems, clinics), payers (insurance carriers, TPAs), health IT companies, pharmaceutical and life sciences organizations, medtech companies, and digital health startups.

Cost depends on scope, regulatory complexity, and integration requirements. A focused clinical tool or patient portal typically ranges from $150K–$400K. Larger platforms with EHR integrations, multi-facility deployment, and compliance certifications typically run $400K–$1.2M+. Every engagement begins with a structured discovery phase where we define scope, identify risks, and establish a realistic budget before development starts.

FHIR (Fast Healthcare Interoperability Resources) is the modern standard for exchanging healthcare data between systems. It replaced older standards like HL7 v2 with a REST-based API approach that's faster to implement, easier to maintain, and required by the 21st Century Cures Act for patient data access. If you're building any system that needs to exchange data with EHRs, labs, pharmacies, or payers, FHIR compliance is effectively mandatory. Our teams build FHIR R4-compliant integrations as standard practice.

Timeline depends on scope and regulatory complexity. A focused clinical tool or patient-facing mobile app might take 4–6 months from discovery through production. Larger platforms with multiple EHR integrations, compliance certifications, and multi-facility deployment typically run 8–14 months with phased delivery — so you see working software early and can validate with real clinical users before full rollout.

We build companion applications and data platforms that interface with medical devices, as well as Software as a Medical Device (SaMD) solutions that require FDA regulatory consideration. Our teams understand the distinction between clinical decision support tools that fall under FDA oversight and general wellness applications that don't. For SaMD projects, we implement quality management system (QMS) processes aligned with FDA guidance and IEC 62304 software lifecycle standards.